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Tert-Butyl nitrite → (4-Bromo-2,3-dimethylphenyl)(methyl)sulfane

HRID 992824
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HRID 992824 반응식
N(OC(C)(C)C)=O.[Br:8][C:9]1[CH:15]=[CH:14][C:12](N)=[C:11]([CH3:16])[C:10]=1[CH3:17].[CH3:18][S:19]SC>[Cu]>[CH3:17][C:10]1[C:11]([CH3:16])=[C:12]([S:19][CH3:18])[CH:14]=[CH:15][C:9]=1[Br:8]
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참가 물질

5

반응물 3

HCID 10906Tert-Butyl nitriteHCID 12232Dimethyl DisulfideHCID 234369094-Bromo-2,3-dimethylaniline

생성물 1

HCID 18757276(4-Bromo-2,3-dimethylphenyl)(methyl)sulfane

시약·촉매·용매 1

HCID 23978Copper촉매

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온도
77.5 °C

실험 절차

603 g (5.85 mol) of tert-butyl nitrite and 375 g of copper powder (5.9 mol) are initially charged in 3000 ml of dimethyl disulfide, and 761 g (3.75 mol) of 4-bromo-2,3-dimethylaniline are added dropwise at from 50 to 58° C. The mixture is subsequently stirred at from 75 to 80° C. for 9 hours. For work-up, the mixture is cooled, the residue is filtered off and the filtrate is washed with saturated aqueous NaHCO3 solution. For purification of the product, the organic phase is separated by distillation. Initially, the excess dimethyl disulfide is separated off at atmospheric pressure. 1870 g of dimethyl disulfide (purity>97% according to GC) are recovered. The residue is subsequently subjected to fractional distillation under reduced pressure (0.1 mbar).

후처리

  1. temperatureFor work-up, the mixture is cooled
  2. filtrationthe residue is filtered off
  3. washthe filtrate is washed with saturated aqueous NaHCO3 solution
  4. customFor purification of the product
  5. customthe organic phase is separated by distillation
  6. customInitially, the excess dimethyl disulfide is separated off at atmospheric pressure
  7. custom1870 g of dimethyl disulfide (purity>97% according to GC) are recovered
  8. distillationThe residue is subsequently subjected to fractional distillation under reduced pressure (0.1 mbar)

출처 및 근거

ORD 기록
ord-eb32376f675745f3b9859a438d80af15
출처 데이터셋
uspto-grants-2002_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06469176B1

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